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Volumn 83, Issue 2, 2005, Pages 452-454

Mayer-Rokitansky-Küster-Hauser syndrome associated with thrombocytopenia-absent radius syndrome

Author keywords

Developmental defect of the genitourinary tract; Mayer Rokitansky K ster Hauser syndrome; Radius aplasia; Thrombocytopenia absent radius syndrome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL MALFORMATION; DIAGNOSTIC PROCEDURE; DISEASE COURSE; FEMALE; HUMAN; LABORATORY TEST; LAPAROSCOPY; OCCUPATIONAL THERAPY; PHYSIOTHERAPY; PLASTIC SURGERY; PRIORITY JOURNAL; ROKITANSKY SYNDROME; THROMBOCYTOPENIA ABSENT RADIUS SYNDROME; TREATMENT OUTCOME;

EID: 13544260715     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2004.06.077     Document Type: Article
Times cited : (30)

References (12)
  • 1
    • 0023864689 scopus 로고
    • Thrombocytopenia with absent radii: A review of 100 cases
    • V.A. Hedberg, J.M. Lipton Thrombocytopenia with absent radii A review of 100 cases Am J Pediatr Hematol Oncol 10 1988 51 64
    • (1988) Am J Pediatr Hematol Oncol , vol.10 , pp. 51-64
    • Hedberg, V.A.1    Lipton, J.M.2
  • 3
    • 0017082529 scopus 로고
    • Congenital absence of the vagina: The Mayer-Rokitansky-Küster-Hauser syndrome
    • J. Griffin, C. Edwards, J. Madden, M. Harrod, J. Wilson Congenital absence of the vagina The Mayer-Rokitansky-Küster-Hauser syndrome Ann Intern Med 85 1976 224 236
    • (1976) Ann Intern Med , vol.85 , pp. 224-236
    • Griffin, J.1    Edwards, C.2    Madden, J.3    Harrod, M.4    Wilson, J.5
  • 4
    • 0028098052 scopus 로고
    • Bilateral femoral hypoplasia associated with Rokitansky sequence: Another example of a mesodermal malformation spectrum?
    • C.H. Bau, C.A. Ribeiro, S.A. Ribeiro, R.Z. Flores Bilateral femoral hypoplasia associated with Rokitansky sequence: another example of a mesodermal malformation spectrum? Am J Med Genet 49 1994 205 206
    • (1994) Am J Med Genet , vol.49 , pp. 205-206
    • Bau, C.H.1    Ribeiro, C.A.2    Ribeiro, S.A.3    Flores, R.Z.4
  • 5
    • 0023224865 scopus 로고
    • Evaluation of radiographic abnormalities of the hand in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
    • E.H. Strubbe, C.J. Thijn, W.N. Willemsen, R. Lappohn Evaluation of radiographic abnormalities of the hand in patients with the Mayer-Rokitansky- Küster-Hauser syndrome Skeletal Radiol 16 1987 227 231
    • (1987) Skeletal Radiol , vol.16 , pp. 227-231
    • Strubbe, E.H.1    Thijn, C.J.2    Willemsen, W.N.3    Lappohn, R.4
  • 7
    • 0030707708 scopus 로고    scopus 로고
    • A conserved Hox axis in the mouse and human female reproductive system: Late establishment and persistent adult expression of the Hoxa cluster genes
    • H.S. Taylor, G.B. Vanden Heuvel, P. Igarashi A conserved Hox axis in the mouse and human female reproductive system: late establishment and persistent adult expression of the Hoxa cluster genes Biol Reprod 57 1997 1338 1345
    • (1997) Biol Reprod , vol.57 , pp. 1338-1345
    • Taylor, H.S.1    Vanden Heuvel, G.B.2    Igarashi, P.3
  • 8
    • 0030002141 scopus 로고    scopus 로고
    • The molecular basis of hypodactyly (Hd): A deletion in Hoxa 13 leads to arrest of digital arch formation
    • D.P. Mortlock, L.C. Post, J.W. Innis The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation Nat Genet 13 1996 284 289
    • (1996) Nat Genet , vol.13 , pp. 284-289
    • Mortlock, D.P.1    Post, L.C.2    Innis, J.W.3
  • 9
    • 0031050961 scopus 로고    scopus 로고
    • Mutation of HOXA13 in hand-foot-genital syndrome
    • D.P. Mortlock, J.W. Innis Mutation of HOXA13 in hand-foot-genital syndrome Nat Genet 15 1997 179 180
    • (1997) Nat Genet , vol.15 , pp. 179-180
    • Mortlock, D.P.1    Innis, J.W.2
  • 10
    • 0030968044 scopus 로고    scopus 로고
    • HOX gene links limb, genital defects
    • S. Dickman HOX gene links limb, genital defects Science 275 1997 1568
    • (1997) Science , vol.275 , pp. 1568
    • Dickman, S.1
  • 11
    • 0036175014 scopus 로고    scopus 로고
    • Absence of mutations in the HoxA10, HoxA11 and HoxD11 nucleotide coding sequences in thrombocytopenia with absent radius syndrome
    • R.A. Fleischman, R. Letestu, X. Mi, D. Stevens, J. Winters, N. Debili Absence of mutations in the HoxA10, HoxA11 and HoxD11 nucleotide coding sequences in thrombocytopenia with absent radius syndrome Br J Haematol 116 2002 367 375
    • (2002) Br J Haematol , vol.116 , pp. 367-375
    • Fleischman, R.A.1    Letestu, R.2    Mi, X.3    Stevens, D.4    Winters, J.5    Debili, N.6
  • 12
    • 0041834837 scopus 로고    scopus 로고
    • Monozygotic twins discordant for vaginal agenesis and bilateral tibial longitudinal deficiency
    • M.P. Steinkampf, S.P. Dharia, R.D. Dickerson Monozygotic twins discordant for vaginal agenesis and bilateral tibial longitudinal deficiency Fertil Steril 80 2003 643 645
    • (2003) Fertil Steril , vol.80 , pp. 643-645
    • Steinkampf, M.P.1    Dharia, S.P.2    Dickerson, R.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.